Evidence map›Paper›PMID 34313339›Full record

ReviewImmunological reviews2021

Biochemical coordination of plasma cell genesis.

Brian T Gaudette, David Allman

Open access · greenAbstract readReview
In one paragraph

Review in Immunological reviews, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 23% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Brian T GaudetteThe Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.ORCID 0000-0001-6627-3085
David AllmanThe Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.ORCID 0000-0001-9345-1502
University of Pennsylvania · US

Funding

IMMUNOBIOLOGY OF NORMAL AND NEOPLASTIC LYMPHOCYTEST32CA009140 · NCI · UNIVERSITY OF PENNSYLVANIA · PI Malay Haldar, WARREN S PEAR · 1985 to 2026
$16.1M
Proteasome Targeting for Alloreactive Plasma CellsR01AI154932 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI ALLMAN, DAVID M, HILDEMAN, DAVID A · 2020 to 2025
$7.2M
Very early plasma cell differentiationR01AI139123 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI ALLMAN, DAVID M, ARGON, YAIR · 2018 to 2022
$3.0M
Long-lived CD19-positive plasma cellsR01AI097590 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI ALLMAN, DAVID M · 2012 to 2016
$1.9M
Control of plasma cell longevity by the IRE1 pathwayR21AI115710 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI ALLMAN, DAVID M, ARGON, YAIR · 2015 to 2016
$458k
Plasma Cell PrimingR21AI133998 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI ALLMAN, DAVID M, CANCRO, MICHAEL PAUL · 2017 to 2018
$443k
National Institute of Allergy and Infectious Diseases R01-AI097590National Institute of Allergy and Infectious Diseases R01-AI154932National Institute of Allergy and Infectious Diseases T32-CA009140NCI NIH HHS T32 CA009140NIAID NIH HHS R01 AI097590NIAID NIH HHS R01 AI139123NIAID NIH HHS R01 AI154932NIAID NIH HHS R21 AI115710NIAID NIH HHS R21 AI133998
6 · The paper itself

Abstract

Antibody-secreting plasma cells are a central component of short- and long-term adaptive immunity. Yet, many fundamental questions about how activated B cells decide to yield functional plasma cells have yet to be answered. Likewise, the biochemical processes underpinning the ability of plasma cells to generate and secrete large numbers of antibodies, the capacity of some plasma cell to sustain antibody secretion, presumably without interruption, for decades, and the capacity of long-lived plasma cells to avoid apoptosis despite the high-energy demands associated with sustained robust antibody synthesis and secretion each remain mysterious processes. Our objective here is to review what is currently known about these processes with an emphasis on the earliest phases of plasma cell genesis. Along the way, we will work toward developing a model that ties the biochemistry of plasma cell function and survival. The chief idea imbedded in this model is that progress toward understanding plasma cell survival mechanisms may require increased focus on the unique cell autonomous processes inherent in plasma cell differentiation and function.

Indexed as

B-LymphocytesPlasma CellsAntibody FormationAntibody-Producing CellsCell DifferentiationLymphocyte ActivationantibodiesB-cellscell differentiationcell lineages and subsetsmoleculesprocesses

Identifiers

PMID34313339
PMCPMC8966904
OpenAlexW3186475405

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.